Angiostrongylus vasorum infection in red foxes (Vulpes vulpes) in southern Italy.

Angiostrongylus vasorum (Nematoda: Angiostrongylidae) infection was detected at post-mortem examination in the pulmonary arteries and hearts of 34/102 (33,3%) of red foxes (Vulpes vulpes) from the Campania Region in southern Italy. Pathological changes consisted of granulomatous interstitial pneumonia caused by larvae and intravascular pulmonary adult nematodes. These changes confirm that angiostrongylosis infection in red foxes has a mainly chronic course, in which the infected host may disperse parasite larvae in the environment over its lifetime. Results suggest that the life cycle of A. vasorum is well established in the red fox in the Campania Region representing a potential infection risk for dogs.

Cosmetic reconstruction of a nasal plane and rostral nasal skin defect using a modified nasal rotation flap in a dog.

OBJECTIVE: To report reconstruction of a defect of the nasal plane and the rostral dorsum of the nose in a dog using a nasal rotation flap with Burow's triangles. STUDY DESIGN: Clinical report. ANIMALS: Mixed-breed dog (1.5 years, 8.6 kg). METHODS: A nasal defect caused by chronic granulomatous inflammation and involving the lateral nasal plane and adjacent rostral nasal dorsum in a dog was reconstructed and closed using a unilateral nasal rotation flap incorporating dorsal nasal plane tissue, with excision of Burow's triangles. RESULTS: The modified unilateral nasal rotation flap was effective in closing a defect of the rostral nasal dorsum. Incorporation of dorsal nasal plane tissue in the flap allowed for a cosmetic reconstruction of the lateral nasal plane defect (wing of nostril). CONCLUSIONS: Skin defects on the rostral dorsum of the nose and defects of the nasal plane in dogs can be closed and/or reconstructed using nasal rotation flaps incorporating nasal plane tissue.

Systemic granulomatous disease and sialometaplasia in a dog with Bartonella infection.

Systemic granulomatous disease involving the spleen, heart, lymph nodes, omentum, liver, kidney, lung, mediastinum, and salivary glands developed in an 8-year-old Rottweiler. The dog also had sialometaplasia of both submandibular salivary glands. Bartonella henselae and B. vinsonii subsp. berkhoffii DNA was amplified from the salivary gland by polymerase chain reaction analysis. Bartonellae may be the cause of this systemic disease, but to the authors' knowledge, involvement of omentum, mediastinum, and salivary glands has not previously been reported in association with Bartonella infection. Bartonellae should be considered potential causes of sialometaplasia.

Three types of immunotherapics against pythiosis insidiosi developed and evaluated.

Pythiosis is a granulomatous disease of horses, cattle, dogs, cats and humans identified in tropical and subtropical areas and caused by Pythium insidiosum, a zoosporic fungus. Experimental models of pythiosis in naturally infected species have not yet been reported but, rabbits may be inoculated with zoospores as an experimental model for studying the disease. The present study evaluates the efficacy of three different of immunotherapics in the rabbit model. Approximately 17500 zoospores of oomycete P. insidiosum (CBS 101555 strain) were inoculated in each animal to generate the disease. Immunotherapics were produced from vortexed or sonicated cultures of the same strain. Four groups of five animals were employed: group 1, placebo; group 2, sonicated immunotherapic; group 3, mixed immunotherapic; and group 4, vortexed immunotherapic. All rabbits were inoculated with viable zoospores one month before administration of the immunotherapics. Eight doses of immunotherapic or placebo were used in each animal with a 14 day interval between injections. Rabbits receiving the vortexed immunotherapic were most effectively protected (P<0.05), showing a decrease in the area of coastal nodules due to Pythiosis insidiosum by 71.8% after 26 weeks of evaluation. Moreover, two animals in this group showed complete remission of the infection at the end of the 26 weeks. In contrast to these findings, rabbits given the sonicated immunotherapic did not show any protection and had an increase of 211.8% in the size of lesions. This failure of sonicated immunotherapic may reflect denaturation of protective antigens due to the sonication method.

Idiopathic systemic granulomatous disease with encephalitis in a horse.

A 14-year-old standardbred mare with clinically suspected acute bronchitis was killed because of rapidly progressing central nervous disturbances. Necropsy revealed systemic granulomatous inflammation and vasculitis involving the lungs, thoracic lymph nodes, ribs, and liver. In the cerebrum there was a severe subacute bilateral encephalitis and malacia predominately affecting the white matter, and vasculitis with perivascular infiltration of lymphocytes, macrophages, and giant cells. A causative infectious agent could not be detected by Ziehl-Neelsen, Grocott, or Giemsa stains, by periodic acid-Schiff reaction of tissue sections, nor by bacterial and fungal cultures. Therefore, idiopathic systemic granulomatous disease (ISGD) was diagnosed and an immune-mediated pathogenesis was suspected. Inflammatory involvement of the brain has hitherto not been reported in cases of equine ISGD. This case seems to be an uncommon variant of ISGD with encephalitis and lack of dermal involvement.

Idiopathic systemic granulomatous disease and macrophage expression of PTHrP in a miniature pony.

Idiopathic systemic granulomatous disease, which has been reported in horses, cattle and human beings, is characterized by perivascular granulomatous and lymphoplasmacytic inflammation in many organ systems. Diagnosis is based on the exclusion of possible viral, fungal or bacterial causes. The disease was identified in a miniature pony with widespread lymphoplasmacytic and granulomatous inflammation, special staining techniques having revealed no evidence of any aetiological agent. Skin lesions, which were severe, consisted of hyperkeratosis and serocellular crust formation, with inflammatory infiltrates in a perivascular to diffuse pattern in both the superficial and deep dermis. Inflammatory infiltrates were also present in lymph nodes and around the blood vessels in most organs. Immunohistochemically, both CD3-positive T lymphocytes and BLA36-positive B lymphocytes were identified in the inflammatory infiltrates, and macrophages were immunolabelled for parathyroid hormone-related protein, a factor associated with hypercalcaemia in human beings with granulomatous diseases.

Pitiose / Pythiosis

A pitiose é uma enfermidade granulomatosa crônica, principalmente do tecido subcutâneo, causada pelo Oomiceto Pythium insidiosum que acomete humanos e animais. A espécie eqüina é a mais atingida, havendo vários relatos da doença no Brasil. A enfermidade destaca-se pela dificuldade de tratamento, representando um risco importante para a vida de animais e humanos afetados. O diagnóstico precoce e correto é fundamental para o sucesso da terapia. A dificuldade de tratamento deve-se à ausência de drogas antifúngicas ativas contra o agente. Recentemente, a imunoterapia tem surgido como uma alternativa terapêutica potencial. Nesse artigo, os aspectos micológicos, epidemiológicos, clínicos e histopatológicos da pitiose nas diferentes espécies säo revisados. As técnicas diagnósticas disponíveis e as perspectivas terapêuticas também säo abordadas.

Bronchopulmonary and disseminated granulomatous disease associated with Aspergillus fumigatus and Candida species infection in a golden retriever.

A seven-year-old, female golden retriever was referred for a paroxysmal, chronic cough and dyspnea, dysphagia, facial pruritus, anterior uveitis, and deteriorating general condition. A severe, mixed interstitial and alveolar pattern, with poorly defined amorphous lesions, was seen on thoracic radiographs. Multiple, whitish nodules disseminated on the hyperemic respiratory mucosa were noted on bronchoscopy. Escherichia coli and Aspergillus fumigatus were cultured from the bronchoalveolar lavage. Granulomatous lesions in numerous organs were identified during necropsy, and Aspergillus fumigatus and Candida spp. were cultured from lung and kidney tissues. Microscopic granulomatous lesions were compatible with mycotic infection; however fungal organisms were not observed.

Histological and topographical characteristics of canine granulomatous leptomeningitis.

Histological and topographical characteristics of granulomatous leptomeningitis were studied in 14 laboratory beagle dogs (12 males, two females), 8 to 19 months old. The dogs, which were either saline-treated controls or drug-treated animals in four different toxicity studies, remained clinically normal during the experimental period, and granulomatous leptomeningitis was identified as an incidental finding by routine histopathological examination. There were no macroscopical lesions in the brain or other organs. Microscopical lesions of the central nervous system were of three types, namely (1) a diffuse inflammatory type, characterized by diffuse infiltration of macrophages, (2) a granulomatous type, characterized by non-caseating granulomas, or (3) a fibrotic type, featuring dense connective tissue. Each of the 14 cases fell into one of three disease phases, early, fulminating and healing. In the early phase, only diffuse inflammatory-type lesions were seen. In the fulminating phase, all three types of lesion were present. In the healing phase, discrete granulomas were relatively few and fibrosis was prominent.

Granulomatous leptomeningitis in beagle dogs.

A granulomatous leptomeningitis was seen in seven laboratory Beagle dogs (four males, three females), 14 to 15 months old, that had been used as control or experimental subjects in a toxicologic study. The dogs were clinically normal during the experimental period. Microscopic lesions were characterized by typical noncaseating granulomas in leptomeninges and slight scattered perivascular cuffing in gray and white matter throughout the central nervous system, with no site of predilection. Although no microorganisms could be found by ordinary light microscopic examination, there was a positive reaction for Escherichia coli antigen in the cytoplasm of macrophages, which corresponded to periodic acid-Schiff-positive, calcium-negative, and iron-negative materials in the granulomas and cuffs. Electron microscopic examination revealed that these materials were large phagolysosomes indicative of abnormal lysosomal function. These findings indicate that at least some cases of canine granulomatous leptomeningitis could be very likely caused by E. coli and represent an entity distinct from classical canine granulomatous meningoencephalitis.

Dexamethasone-induced recrudescence of malignant catarrhal fever and associated lymphosarcoma and granulomatous disease in a Formosan sika deer (Cervus nippon taiouanus).

Malignant catarrhal fever (MCF) was diagnosed in a 2-week-old Formosan sika deer. The fawn had been previously exposed to a clinically normal neonatal wildebeest calf from which alcelaphine herpesvirus-1 was isolated. Alcelaphine herpesvirus-1 was isolated from buffy coat leukocytes and nasal and ocular secretions of the fawn during the acute illness. The fawn clinically recovered after 3 weeks. Virus was not recovered from blood at this time. Dexamethasone, given 4 months after clinical recovery, resulted in reisolation of MCF virus from blood and recrudescence of clinical MCF. The deer was euthanatized. At necropsy, pathognomonic lesions of MCF, granulomatous disease, and malignant lymphoma were observed. Antibodies to bovine leukosis viral antigens were not detected in the serum. The epidemiologic and pathogenetic importance of the findings are discussed.